Comparison of Continuous Epidural Infusion of Bupivacaine and Fentanyl versus Patient Controlled Analgesia techniques for Labor Analgesia
Phase 2
- Conditions
- Condition 1: Labor pain. Condition 2: delivery.Single spontaneous deliveryMultiple delivery
- Registration Number
- IRCT2014121610765N6
- Lead Sponsor
- Vice chancellor for reaserch, Tabriz University of Medical Scienses
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Inclusion Criteria: Parturients with 18-40 years of old; parturients with ASA Class I or II; consenting to be including to the study; women with active labor and vertex presentation
Exclusion criteria: Parturients with ASA Class III or higher; cardiovascular diseases; respiratory diseases; contraindication for epidural ; presentation other than vertex; patients with chronic pain and use of analgesics; diabetics
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: every 30 minutes from drug adminstration until delivery. Method of measurement: visual analog scale.
- Secondary Outcome Measures
Name Time Method Motor block. Timepoint: every 30 minute from drug adminstration to delivery. Method of measurement: Modified Bromage scale.